Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms.
about
A method for measuring electrical signals in a primary ciliumCEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathiesCiliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19Ex vivo modeling of chemical synergy in prenatal kidney cystogenesisRole of endothelial nitric oxide synthase VNTR (intron 4 a/b) polymorphism on the progression of renal disease in autosomal dominant polycystic kidney diseaseCby1 promotes Ahi1 recruitment to a ring-shaped domain at the centriole-cilium interface and facilitates proper cilium formation and function.Placental mesenchymal dysplasia and fetal renal-hepatic-pancreatic dysplasia: androgenetic-biparental mosaicism and pathogenesis of an autosomal recessive disorder.Mechanism of cystogenesis in nephrotic kidneys: a histopathological study.The spectrum of polycystic kidney disease in children.Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent PolydactylyA TRPM4-dependent current in murine renal primary cilia.Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity.Arl13b and the exocyst interact synergistically in ciliogenesisCentrosomes and cilia in human disease.Keeping the balance between proliferation and differentiation: the primary ciliumMammalian target of rapamycin and the kidney. II. Pathophysiology and therapeutic implications.Birt-Hogg-Dubé syndrome and the skin.Chemical and Physical Sensors in the Regulation of Renal Function.Bardet-Biedl syndrome: Is it only cilia dysfunction?Clinical and ultrasonographical characterization of childhood cystic kidney diseases in Egypt.Large-scale RNA-Seq Transcriptome Analysis of 4043 Cancers and 548 Normal Tissue Controls across 12 TCGA Cancer Types.Increased prevalence of simple renal cysts in patients with gout.Urologic Diseases Germane to the Medical Renal Biopsy: Review of a Large Diagnostic Experience in the Context of the Renal Architecture and Its EnvironsOrphan Kidney Diseases
P2860
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P2860
Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms.
@ast
Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms.
@en
type
label
Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms.
@ast
Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms.
@en
prefLabel
Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms.
@ast
Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms.
@en
P2860
P1433
P1476
Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms.
@en
P2093
Cecilia Gascue
P2860
P2888
P304
P356
10.1007/S00467-010-1697-5
P577
2010-11-27T00:00:00Z